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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264630Generated: November 1, 2026

Triethylamine → 1-[[3-[[2,2-Dicyano-1-[(2-methyl-5-benzofuranyl)amino]ethenyl]amino]-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepin-1-yl]acetyl]pyrrolidine

https://huagongshe.com/reaction/1264630

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Methyl-5-benzofuranamineHCID 3157484—
Reactant1-[(3-amino-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepin-1-yl)acetyl]pyrrolidineHCID 18612553—
Reactant2-((Methylthio)methylene)malononitrileHCID 18979789—
SolventEthanolHCID 702—
Product1-[[3-[[2,2-Dicyano-1-[(2-methyl-5-benzofuranyl)amino]ethenyl]amino]-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepin-1-yl]acetyl]pyrrolidineHCID 186126173%

Reaction Conditions

Temperature80 °C

Reaction Steps

Preparation of title compound. A solution of 2-methyl-5-benzofuranamine (0.24 mmol), 1,1-bis(methylthio-2,2-dicyanoethylene (34 mg, 0.20 mmol) and triethylamine (0.035 mL, 0.25 mmol) in ethanol (0.35 mL) was stirred at 80° C. for 4 h. To the mixture was added 1-[(3-amino-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepin-1-yl)acetyl]pyrrolidine (70 mg, 0.24 mmol) and the resulting reaction was stirred at 80° C. overnight. The reaction mixture was purified by column chromatography (silica, 5% methanol/ethyl acetate) to afford the title compound (3 mg, 3% yield): MS (ESI, pos. ion spectrum) m/z 509; HPLC (method A) tR 3.80 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06544981B2
Source datasetuspto-grants-2003_04
ORD IDord-0ae0cd8413b64588ae4897cb0b3a898c
Source noteuspto-grants-2003_04